1A30
HIV-1 PROTEASE COMPLEXED WITH A TRIPEPTIDE INHIBITOR
Summary for 1A30
| Entry DOI | 10.2210/pdb1a30/pdb |
| Descriptor | HIV-1 PROTEASE, TRIPEPTIDE GLU-ASP-LEU (3 entities in total) |
| Functional Keywords | aspartic protease, hiv protease, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
| Biological source | Human immunodeficiency virus 1 |
| Cellular location | Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P04585 |
| Total number of polymer chains | 3 |
| Total formula weight | 21984.99 |
| Authors | Louis, J.M.,Dyda, F.,Nashed, N.T.,Kimmel, A.R.,Davies, D.R. (deposition date: 1998-01-27, release date: 1998-04-29, Last modification date: 2024-02-07) |
| Primary citation | Louis, J.M.,Dyda, F.,Nashed, N.T.,Kimmel, A.R.,Davies, D.R. Hydrophilic peptides derived from the transframe region of Gag-Pol inhibit the HIV-1 protease. Biochemistry, 37:2105-2110, 1998 Cited by PubMed: 9485357DOI: 10.1021/bi972059x PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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